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Weekend Clinical Research Jobs in Highlands Ranch, CO

Clinical Research Coordinator

Aurora, CO · On-site

$24.75 - $32.75/hr

Clinical Research Coordinator Position #: 00851764 - Requisition #: 40742 Job Summary: The Division ... Flexible work hours, including infrequent evenings or weekends, may be required. This position ...

Clinical Research Coordinator

Aurora, CO · On-site

$24.75 - $32.75/hr

Clinical Research Coordinator Position #: 00851764 - Requisition #: 40742 Job Summary: The Division ... Flexible work hours, including infrequent evenings or weekends, may be required. This position ...

About Us: CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of ...

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Weekend Clinical Research information

See Highlands Ranch, CO salary details

$51.4K

$112.7K

$198.4K

How much do weekend clinical research jobs pay per year?

As of Aug 30, 2026, the average yearly pay for weekend clinical research in Highlands Ranch, CO is $112,661.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $128,600.00 per year, depending on experience, location, and employer.

What is a weekend clinical research?

A Weekend Clinical Research job involves conducting or supporting clinical trials on weekends, typically for medical or pharmaceutical research. Responsibilities may include patient recruitment, data collection, monitoring study protocols, and ensuring regulatory compliance. These roles are ideal for professionals looking for flexible work schedules while contributing to medical advancements. Weekend clinical research positions are often available at hospitals, research institutions, or pharmaceutical companies.

What are the key skills and qualifications needed to thrive in weekend clinical research?

To thrive in Weekend Clinical Research, you need a background in life sciences or healthcare, experience in clinical trial processes, and attention to detail. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and proficiency in using Microsoft Office Suite are often required. Strong organizational skills, effective communication, and the ability to work independently during off-hours are key soft skills. These capabilities are crucial to ensure accurate data collection, adherence to regulatory standards, and smooth collaboration with research teams outside standard work hours.

What does a typical weekend schedule look like for weekend clinical research?

Weekend Clinical Research roles often involve supporting ongoing clinical trials by assisting with patient visits, data entry, and documentation tasks that must be completed outside of regular business hours. You may work independently or as part of a small team, coordinating closely with principal investigators and other study staff to ensure continuity and compliance with study protocols. Flexibility and reliability are important, as your work ensures that weekend operations integrate seamlessly with weekday research activities. This role is ideal for candidates looking for part-time opportunities or those balancing other weekday commitments with their passion for clinical research.

What are the most commonly searched types of Clinical Research jobs in Highlands Ranch, CO?

The most popular types of Clinical Research jobs in Highlands Ranch, CO are:

What are popular job titles related to Weekend Clinical Research jobs in Highlands Ranch, CO?

For Weekend Clinical Research jobs in Highlands Ranch, CO, the most frequently searched job titles are:

What job categories do people searching Weekend Clinical Research jobs in Highlands Ranch, CO look for?

The top searched job categories for Weekend Clinical Research jobs in Highlands Ranch, CO are:

What cities near Highlands Ranch, CO are hiring for Weekend Clinical Research jobs?

Cities near Highlands Ranch, CO with the most Weekend Clinical Research job openings:

Clinical Research Coordinator

ECN Operating LLC

Denver, CO

$25 - $33.25/hr

Full-time

Re-posted 6 days ago


Job description

Job Summary:

We are seeking a highly organized and motivated Clinical Research Coordinator (CRC) to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred, as this role may include specimen collection and basic clinical procedures.

Key Responsibilities:

  • Coordinate day-to-day clinical research activities to ensure study protocols are followed.
  • Recruit, screen, and enroll study participants.
  • Obtain informed consent and ensure ethical conduct in all study interactions.
  • Collect, process, and ship biological specimens per protocol (e.g., blood draws, urine samples).
  • Perform basic clinical procedures as permitted by certification (e.g., vital signs, EKGs).
  • Maintain accurate and timely documentation in case report forms and electronic databases.
  • Communicate with sponsors, monitors, and IRBs regarding study progress and compliance.
  • Schedule participant visits and follow-ups; ensure visit windows are met.
  • Ensure proper storage, handling, and accountability of investigational products, if applicable.
  • Maintain regulatory documents and assist with IRB submissions.

Qualifications:

  • Bachelor's degree in a health-related field required.
  • At least 1–2 years of experience in clinical research preferred.
  • Phlebotomy certification or MA certification preferred.
  • Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
  • Excellent organizational skills and attention to detail.
  • Strong interpersonal and communication skills.
  • Proficiency in Microsoft Office and electronic data capture systems (e.g., REDCap, EDC platforms).
  • Ability to work independently and as part of a multidisciplinary team.

Preferred Qualifications:

  • Experience working in clinical trials, especially in a hospital or academic setting.
  • Familiarity with IRB processes and clinical trial documentation.
  • Bilingual skills (depending on patient population) may be a plus.

Job Type: Full-time

Work Location: In person

Schedule:

  • 8 hour shift
  • Monday to Friday
  • Weekends as needed